CREB1-induced miR-1204 promoted malignant phenotype of glioblastoma through targeting NR3C2.

BACKGROUND: Glioblastoma (GBM) is a subclass of brain malignancy with unsatisfactory prognosis. MicroRNAs (miRNAs) are a group of non-coding RNAs (ncRNAs) that exert key function on tumorigenesis and tumor development. PURPOSES: The purpose of this work was to unravel the biological behavior and mechanism of miR-1204 in GBM. METHODS: Expressions of miR-1204, NR3C2 and CREB1 were detected by RT-qPCR and western blot. Proliferation and apoptosis of GBM cells were detected by CCK-8, colony formation, caspase-3 activity and TUNEL assays. Molecular interplays were examined by ChIP, RIP, and luciferase reporter assays. RESULTS: MiR-1204 level was elevated in GBM cell lines. Functionally, miR-1204 aggravated cell proliferation whereas suppressed cell apoptosis in GBM cells. Mechanistically, cAMP Responsive Element Binding Protein 1 (CREB1) bound to the promoter of miR-1204 and activated the transcription of miR-1204. Furthermore, miR-1204 targeted and inhibited Nuclear receptor subfamily 3 group C member 2 (NR3C2), a tumor suppressor gene in GBM cells. Rescue assays indicated that NR3C2 participated in the regulation of miR-1204 on the malignant phenotype of GBM cells. CONCLUSIONS: We observed for the first time that CREB1-induced miR-1204 promoted malignant phenotype of GBM through targeting NR3C2, indicating that miR-1204 acted as a novel oncogenic miRNA in GBM.

Adsorption of crystal violet on activated bamboo fiber powder from water: preparation, characterization, kinetics and isotherms.

Biomass-activated carbon has made a great contribution as an adsorbent in the field of dye wastewater treatment. In this study, the response surface method (RSM) based on the Box-Behnken design was used to optimize the preparation process. Bamboo fiber activated carbon (BAC) with a specific surface area of 2892 m2 g-1 and a pore volume of 1.80 cm3 g-1 was prepared. Various characterization methods (SEM, XPS, XRD, and Raman spectroscopy) were used to analyze the micro-structure of BAC. In the microscopic state, the BAC is fibrous and maintains the originally connected pores of the bamboo fiber. After high-temperature activation, the microcrystallinity of BAC decreases, and the degree of graphitization is low, indicating the presence of amorphous carbon. The adsorption capacity of BAC to crystal violet in simulated wastewater was evaluated via an adsorption experiment. Under the following conditions: the dosage of BAC was 0.04 g, the concentration was 600 mg L-1, the adsorption temperature and time were 25 °C and 30 min, respectively, and the as-prepared BAC had a 99.96% removal rate. The adsorption process conformed to the pseudo-second-order kinetic model and Langmuir adsorption isotherm model, indicating that the adsorption process of CV on BAC belonged to monomolecular layer adsorption. The adsorption process occurs spontaneously and is accompanied by heat release, and the maximum adsorption capacity of BAC within a given concentration range could reach 1353.09 mg g-1. SEM-EDS characterization before and after adsorption showed that ion exchange and the presence of oxygen-containing functional groups played an important role in promoting the adsorption process. The results show that BAC considerably affects CV removal, which has great application prospects.

Generation and characterization of coal-based needle coke produced by the co-carbonization of coal liquefaction pitch and anthracene oil.

In this study, we studied the feasibility of preparing high-quality needle coke from coal liquefaction pitch. Nine types of blending pitch (coal liquefaction pitch and anthracene oil mixed with different ratios) were used as raw materials to generate needle coke via the co-carbonization method. Optical microscopy, X-ray diffraction, Raman spectroscopy and scanning electron microscopy were employed to determine the properties (microstructure, distribution of carbon microcrystals, true density and micro-strength) of the needle coke derived by the co-carbonization method. Actually, the co-carbonization of coal liquefaction pitch and anthracene oil was an essential method to control the micro-structure and property of the derived needle coke. Briefly, the needle coke derived by the co-carbonization of coal liquefaction pitch and anthracene oil had a lower content of mosaic structure of 14.17%, ideal carbon crystal content of 82.67%, and true density of 2.296 g cm-3. Briefly, the addition of anthracene oil is a suitable method to adjust the property of coal liquefaction pitch, which is also a good method to produce high-quality needle coke via the co-carbonization of coal liquefaction pitch and anthracene oil. Thus, the use of coal liquefaction pitch and anthracene oil as raw materials to generate high-quality needle coke is a considerable method to realize the clean and high value-added utilization of coal liquefaction pitch.

On-off-on nanosensors of carbon quantum dots derived from coal tar pitch for the detection of Cu2+, Fe3+, and L-ascorbic acid.

Novel nitrogen-doped carbon quantum dots (N-CQDs) were synthesized by a chemical oxidation method using medium-low temperature coal tar pitch as the raw material. Such quantum dots were developed as a highly sensitive fluorescent "on-off-on" switch sensor for the selective and simultaneous sensing of Cu2+ and Fe3+. The as-prepared N-CQDs, which emit blue light, were characterized by TEM images, FT-IR spectra, Raman spectroscopy, XPS analysis, fluorescence spectra, and UV-vis absorption spectra. The results showed that the N-CQDs exhibit outstanding optical properties and high optical stability within the pH range of 4-10, with a quantum yield of approximately 7%. Additionally, the material performed as an "on-off" sensor which can be dramatically extinguished by Cu2+ and Fe3+. A linear relationship between Cu2+ and Fe3+ ion concentration and fluorescence intensity was observed in the range from 0 to 50 µM. The limits of detection of the fluorescent sensor toward Cu2+ and Fe3+ were 0.16 µM and 0.173 µM, respectively. The Fe3+-quenched N-CQDs were restored after adding L-ascorbic acid, due to the redox reaction between Fe3+ and L-ascorbic acid, which resulted in the detachment of Fe3+ from the surface of the N-CQDs. The linear range for the detection of L-ascorbic acid was 0-28 µM. Therefore, the amount of L-ascorbic acid can be measured by using the sensing system consisting of Fe3+ and N-CQDs. In consequence, N-CQDs are considered an important material for the detection of Cu2+ and Fe3+ in water samples or L-ascorbic acid in drugs.